Menadione‐induced caspase‐dependent programmed cell death in the green chlorophyte Chlamydomonas reinhardtii. Issue 3 (6th May 2014)

• Record Type: Journal Article
• Authors: Sirisha, V. L.; Sinha, Mahuya; D'Souza, Jacinta S.; Cock, M.
• Is Part Of: Journal of phycology. Volume 50:Issue 3(2014:Jun.)
• Page Start: 587
• Page End: 601
• Publication Date: 2014-05-06
• Subjects: Algae -- Periodicals; 579.8
• DOI: 10.1111/jpy.12188
• Languages: English
• ISSNs: 0022-3646

Abstract

<abstract abstract-type="main" id="jpy12188-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Menadione, a quinone that undergoes redox cycles leading to the formation of superoxide radicals, induces programmed cell death (PCD) in animals and plants. In this study, we investigated whether the unicellular green alga <italic>Chlamydomonas reinhardtii</italic> P.A.Dangeard is capable of executing PCD upon exposure to menadione stress. We report here, the morphological, molecular, and biochemical changes after menadione exposure of <italic>C. reinhardtii</italic> cells. The effect of menadione on cell death has been shown to be dose‐dependent; 5–100 μM menadione causes 20%–46% cell death, respectively. It appears that growth is inhibited with the concomitant degradation of the photosynthetic pigments and by a decrease in the photosynthetic capacity. Being an oxidative stress, we found an H<sub>2</sub>O<sub>2</sub> burst within 15 min of menadione exposure, followed by an increase in antioxidant enzyme (superoxide dismutase [SOD], catalase [CAT], and ascorbate peroxidase [APX]) activities. In parallel, RT‐PCR was performed for transcript analyses of <italic>Mn‐SOD</italic>, <italic> CAT</italic><sub><italic>, </italic></sub> and <italic>APX</italic>. Our results clearly revealed that expression of these genes were up‐regulated upon menadione exposure. Furthermore, classical hallmarks of PCD such as alteration of mitochondrial membrane potential, significant increase in caspase‐3‐like DEVDase activity, cleavage of poly (ADP) ribose polymerase (PARP)‐1‐like enzyme, and DNA fragmentation as detected by terminal deoxynucleotidyl transferase‐mediated dUTP nick end‐labeling (TUNEL) assay and oligosomal DNA fragmentation were observed. Moreover, antibodies against a mammalian active caspase‐3 shared epitopes with a caspase‐3‐like protein of ~17 kDa; its pattern of expression and activity correlated with the onset of cell death. To the best of our knowledge, this is the first report on menadione‐induced PCD through a mitochondrian‐caspase protease pathway in an algal species.</p> </abstract>